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510(k) Data Aggregation
K Number
K970113Device Name
ULTRA-BLEND PLUSManufacturer
Date Cleared
1997-04-02
(79 days)
Product Code
Regulation Number
872.3250Type
TraditionalPanel
DentalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
ULTRA-BLEND PLUS
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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